Environmental implications, potential value, and future of food-waste anaerobic digestate management: A review.

Globally, the valorisation of food waste into digestate through the process of anaerobic digestion is becoming increasingly popular. As a result, a large amount of food-waste digestate will need to be properly utilised. The utilisation of anaerobic digestion for fertiliser and alternative uses is essential to obtain a circular bioeconomy. The review aims to examine the environmental management of food-waste digestate, the value of digestate as a fertiliser and soil conditioner, and the emerging uses and improvements for post-anaerobic digestion reuse of digestate. Odour emissions, contaminants in food waste, emission and leaching of nutrients into the environment, and the regulations, policies, and voluntary initiatives of anaerobic digestion are evaluated in the review. Food-waste digestate can provide essential nutrients, carbon, and bio-stimulants to soils and increase yield. Recently, promising research has shown that digestates can be used in hydroponic systems and potentially replace the use of synthetic fertilisers. The integration of anaerobic digestion with emerging uses, such as extraction of value-added products, algae cultivation, biochar and hydrochar production, can further reduce inhibitory sources of digestate and provide additional economic opportunities for businesses. Moreover, the end-product digestate from these technologies can also be more suitable for use in soil application and hydroponic use.

Adsorption of As(V) and Ni(II) by Fe-Biochar composite fabricated by co-pyrolysis of orange peel and red mud.

This study aimed to compare the adsorption performance of Fe-biochar composites (Fe-C-N2 and Fe-C-CO2), fabricated by co-pyrolysis of red mud and orange peel in N2 and CO2, for As(V) and Ni(II). By the syngas production comparison test, it was confirmed that CO2 was more advantageous than N2 as a pyrolytic medium gas to produce more CO. The resulting Fe-biochar composite showed the aggregate morphology consisting of different Fe phases (magnetite or metal Fe) from the inherent hematite phase in red mud and carbonized carbon matrix, and there was no distinct difference between the structural shapes of two Fe-biochar composites. Adsorption experiments showed that the adsorption capacities for As(V) and Ni(II) in single mode were almost similar with 7.5 and 16.2 mg g-1 for Fe-C-N2 and 5.6 and 15.1 mg g-1 for Fe-C-CO2, respectively. The adsorption ability of Fe-C-CO2 for both As(V) and Ni(II) was further enhanced in binary adsorption mode (As(V): 13.4 mg g-1, Ni(II):17.6 mg g-1) through additional removal of those ions by Ni(II)-As(V) complexation. The overall results demonstrated CO2-assisted pyrolysis can provide a viable platform to convert waste materials into fuel gases and environmental media for co-adsorption of cationic and anionic heavy metals.

Preparation of nitrogen-doped Cu-biochar and its application into catalytic reduction of p-nitrophenol.

Nitrogen-doped copper-biochar (N-Cu-biochar) was synthesized via pyrolysis of glucose in the presence of copper and melamine and used as a catalyst in the reduction of p-nitrophenol by NaBH4. N-Cu-biochar was characterized by field emission scanning electron microscopy/energy-dispersive spectroscopy, Raman spectroscopy, X-ray Diffraction, and Brunauer-Emmett-Teller surface analyzer. The catalytic performance of N-Cu-biochar was evaluated under varying conditions of NaBH4 concentration, biochar dosage, and initial p-nitrophenol concentration. N-Cu-biochar was composed of ~83% C, ~9% O, and ~8% Cu, with Cu/Cu2O phases evenly dispersed on graphitic carbon aggregates possessing both macro- and meso-pores. N-Cu-biochar showed superior catalytic ability in mediating p-nitrophenol reduction as compared to Cu-biochar and N-doped biochar, achieving complete reduction of 0.35 mM p-nitrophenol within 30 min at a dose of 0.25 g L-1. Reduction of p-nitrophenol catalyzed by N-Cu-biochar followed pseudo-first-order kinetics, and the reaction rate was dependent upon NaBH4 concentration. The overall results indicate that biochar can be a suitable candidate as a support for catalyst synthesis, and N-doped Cu-biochar can be a promising catalyst for the reduction of p-nitrophenol.

Exploring potential applications of a novel extracellular polymeric substance synthesizing bacterium (Bacillus licheniformis) isolated from gut contents of earthworm (Metaphire posthuma) in environmental remediation.

The aim was to isolate, characterize, and explore potentials of gut bacteria from the earthworm (Metaphire posthuma) and imply these bacteria for remediation of Cu(II) and Zn(II). An extracellular polymeric substance (EPS) producing gut bacteria (Bacillus licheniformis strain KX657843) was isolated and identified based on 16S rRNA sequencing and phylogenetic analysis. The strain showed maximum tolerance of 8 and 6 mM for Cu(II) and Zn(II) respectively. It removed 34.5% of Cu(II) and 54.4% of Zn(II) at 25 mg L-1 after 72 and 96 h incubation respectively. The bacteria possessed a great potential to produce indole acetic acid (38.49 µg mL-1) at 5 mg mL-1 L-tryptophan following 12 days incubation. The sterilized seeds of mung beans (Vigna radiata) displayed greater germination and growth under bacterium enriched condition. We observed that the bacterial strain phosphate solubilization ability with a maximum of 204.2 mg L-1 in absence of Cu(II) and Zn(II). Endowed with biosurfactant property the bacterium exhibited 24% emulsification index. The bacterium offered significant potential of plant growth promotion, Cu(II) and Zn(II) removal, and as such this study is the first report on EPS producing B. licheniformis KX657843 from earthworm which can be applied as powerful tool in remediation programs of Cu(II) and Zn(II) contaminated sites.

Multi-metal resistance and plant growth promotion potential of a wastewater bacterium Pseudomonas aeruginosa and its synergistic benefits.

Water and soil pollution by toxic heavy metals (HMs) is increasing globally because of increase in population, industrialization and urbanization. It is a burning problem for the public, scientists, academicians and politicians how to tackle the toxic contaminants which jeopardize the environment. One possible solution for pollution abatement is a bioremediation-effective and innovative technology that uses biological systems for treatment of contaminants. Many bacteria synthesize indole-3-acetic acid (IAA) which is a product of L-tryptophan metabolism and belongs to the auxin class of plant growth-promoting hormone. The present study aimed at assessing the resistance pattern of wastewater bacteria against multiple HMs and plant growth promotion activity associated with IAA. A Gram-negative bacterial strain Pseudomonas aeruginosa KUJM was isolated from Kalyani Sewage Treatment Plant. This strain showed the potential to tolerate multiple contaminations such as As(III) (50 mM), As(V) (800 mM), Cd (8 mM), Co (18 mM), Cu (7 mM), Cr (2.5 mM), Ni (3 mM) and Zn (14 mM). The capability of IAA production at different tryptophan concentration (1, 2, 5 and 10 mg mL-1) was determined, and seed germination-enhancing potential was also estimated on lentil (Lens culinaris). Such type of HM-resistant, IAA-producing and seed germination-enhancing P. aeruginosa KUJM offer great promise as inoculants to promote plant growth in the presence of toxic HMs, as well as plant inoculant systems useful for phytoremediation of polluted soils. Hence, P. aeruginosa KUJM finds significant applications in HM-contaminated poor agricultural field as well as in bioremediation of HM-contaminated wastewater system.

Improved energy recovery from yard waste by water-starved hydrothermal treatment: Effects of process water and pressure.

This study investigated the feasibility of a high-loading process with less water consumption for the valorization of wet biomass waste through hydrothermal carbonization (HTC) with and without N2 pressurization from the views of water saving, carbon utilization, and energy recovery. The results revealed that reducing the liquid-to-solid ratio from 10 to 2.5 significantly improved carbon storage in hydrochar due to preferential carbon sequestration as the solid phase (59.9%) instead of being lost in the liquid phase (∼10%). The pressurized HTC process resulted in a higher stability hydrochar through the devolatilization of secondary char that was less stable, yet resulted in âˆ¼10% 15% more carbon transformation to the gas phase. A cost-benefit analysis further demonstrated the potential of the high-loading HTC process for enhancing energy recovery while minimizing energy consumption during hydrochar production from high-moisture yard waste.

Nanoparticles modulate heavy-metal and arsenic stress in food crops: Hormesis for food security/safety and public health.

Heavy metal and arsenic (HM-As) contamination at the soil-food crop interface is a threat to food security/safety and public health worldwide. The potential ecotoxicological effects of HM-As on food crops can perturb normal physiological, biochemical, and molecular processes. To protect food safety and human health, nanoparticles (NPs) can be applied to seed priming and soil amendment, as 'manifestation of hormesis' to modulate HM-As-induced oxidative stress in edible crops. This review provides a comprehensive overview of NPs-mediated alleviation of HM-As stress in food crops and resulting hormetic effects. The underlying biochemical and molecular mechanisms in the amelioration of HM-As-induced oxidative stress is delineated by covering the various aspects of the interaction of NPs (e.g., magnetic particles, silicon, metal oxides, selenium, and carbon nanotubes) with plant microbes, phytohormone, signaling molecules, and plant-growth bioregulators (e.g., salicylic acid and melatonin). With biotechnical advances (such as clustered regularly interspaced short palindromic repeats (CRISPR) gene editing and omics), the efficacy of NPs and associated hormesis has been augmented to produce "pollution-safe designer cultivars" in HM-As-stressed agriculture systems. Future research into nanoscale technological innovations should thus be directed toward achieving food security, sustainable development goals, and human well-being, with the aid of HM-As stress resilient food crops.

Practical approach of As(V) adsorption by fabricating biochar with low basicity from FeCl3 and lignin.

One of the main challenges of biochar application for environmental cleanup is rise of pH in water or soil due to high ash and alkali metal contents in the biochar. While this intrinsic property of biochar is advantageous in alleviating soil and water acidity, it severely impairs the affinity of biochar toward anionic contaminants such as arsenic. This study explored a technical approach that can reduce the basicity of lignin-based biochar by utilizing FeCl3 during production of biochar. Three types of biochar were produced by co-pyrolyzing feedstock composed of different combinations of lignin, red mud (RM), and FeCl3, and the produced biochar samples were applied to adsorption of As(V). The biochar samples commonly possessed porous carbon structure embedded with magnetite (Fe3O4) particles. The addition of FeCl3 in the pyrolysis feedstock had a notable effect on reducing basicity of the biochar to yield significantly lower solution pH values than the biochar produced without FeCl3 addition. The extent of As(V) removal was also closely related to the final solution pH and the greatest As(V) removal (>77.6%) was observed for the biochar produced from co-pyrolysis of lignin, RM, and FeCl3. The results of adsorption kinetics and isotherm experiments, along with x-ray spectroscopy (XPS), strongly suggested adsorption of As(V) occurred via specific chemical reaction (chemisorption) between As(V) and Fe-O functional groups on magnetite. Thus, the overall results suggest the use of FeCl3 is a feasible practical approach to control the intrinsic pH of biochar and impart additional functionality that enables effective treatment of As(V).

The determining factors of sediment nutrient content and stoichiometry along profile depth in seasonal water.

In the recent decades, the area of seasonal water (SEW) has substantially increased at the global scale. To evaluate nutrient dynamics in aquatic ecosystems, previous studies have analyzed the determining factors of sediment nutrient content and stoichiometry on whole sediment profiles without depth separation on SEW sites. Such a methodology assumes that SEW sediment is a uniform unit and its nutrient dynamics are regulated by the same mechanism at various depths (uniformity assumption). We tested this assumption using sediment samples from six depth increments of 154 sediment profiles (1 m depth) on SEW sites at Shengjin Lake in subtropical China. We measured sediment total nitrogen (STN), total phosphorus (STP), nutrient fractions, and the molar ratio of STN to STP (RSNP), and investigated their determining factors at various depths. STN, STP, and RSNP were averaged at 1.34 g/kg, 0.55 g/kg, and 5.43, respectively, and all gradually decreased with depth. STN was positively affected by moisture and flooding duration in all depth increments. Instead, the major determining factors of STP changed from particle size at 0-20 cm of depth to pH and electrical conductivity at 30-100 cm of depth. These vertical patterns have close connections with sediment nutrient fractions since sediment N fractions did not shift along profile depths (i.e., over 99 % of STN was organic N) but sediment P fractions did (the percentage of Fe-P and Al-P decreased by 6.25 % but those of Ca-P increased by 4.31 % along the sediment depth gradient). The major determining factors of RSNP showed no obvious vertical patterns because they frequently varied along depth gradients. The results demonstrate that SEW sediment is not a uniform unit and the determining factors of nutrient dynamics change with depth. Our study highlights the importance of improved methodological reflection in studies addressing sediment nutrient dynamics on SEW sites.

Carbon dioxide-assisted thermochemical conversion of magnetically harvested harmful algae into syngas and metal biochar.

With rising of harmful algae blooming and toxin exposure, practical utilization of harmful algae has been developed. This work aimed to magnetically harvest Microcystis aeruginosa (MA) using iron oxides and investigate the feasibility of algae/iron oxides mixture as feedstock in pyrolytic platform to produce syngas and metal biochar. Carbon dioxide (CO2) was used as a feeding gas to enhance the production efficiency of syngas and also functioned pH controller for better MA harvesting and toxin removal. CO2 support brought multiple benefits: magnetite (Fe3O4) and maghemite (γ-Fe2O3) recovered MA in a relatively short period of time (∼1 min), the recovered biomass generated 34-fold increased carbon monoxide, and metal biochar adsorbed higher amount of toxin from MA (2.8-fold). Pyrolytic utilization of harmful algae supported by CO2 and iron oxides could be one of promising techniques for evolution of metal biochar to remove toxin, while efficiently recover biomass and enhance syngas production.

Impacts of land uses on spatio-temporal variations of seasonal water quality in a regulated river basin, Huai River, China.

Land use impacts from agriculture, industrialization, and human population should be considered in surface water quality management. In this study, we utilized an integrated statistical analysis approach mainly including a seasonal Mann-Kendall test, clustering analysis, self-organizing map, Boruta algorithm, and positive matrix factorization to the assessment of the interactions between land use types and water quality in a typical catchment in the Huai River Basin, China, over seven years (2012-2019). Spatially, water quality was clustered into three groups: upstream, midstream, and downstream/mainstream areas. The water quality of upstream sites was better than of mid-, down-, and mainstream. Temporally, water quality did not change significantly during the study period. However, the temporal variation in water quality of up-, down-, and mainstream areas was more stable than in the midstream. The interactions between land use types and water quality parameters at the sub-basin scale varied with seasons. Increasing forest/grassland areas could substantially improve the water quality during the wet season, while nutrients such as phosphorus from cropland and developed land was a driver for water quality deterioration in the dry season. Water area was not a significant factor influencing the variations of ammonia nitrogen (NH3-N) and total phosphorus (TP) in the wet or dry season, due to the intensive dams and sluices in study area. The parameters TP, and total nitrogen (TN) were principally linked with agricultural sources in the wet and dry seasons. The parameters NH3-N in the dry season, and chemical oxygen demand (CODCr) in the wet season were mainly associated with point source discharges. Agricultural source, and urban point source discharges were the main causes of water quality deterioration in the study area. Collectively, these results highlighted the impacts of land use types on variations of water quality parameters in the regulated basin.

Adsorption of potentially harmful elements by metal-biochar prepared via Co-pyrolysis of coffee grounds and Nano Fe(III) oxides.

Nano Fe(III) oxide (FO) was used as an amendment material in CO2-assisted pyrolysis of spent coffee grounds (SCG) and its impacts on the syngas (H2 & CO) generation and biochar adsorptive properties were investigated. Amendment of FO led to 153 and 682% increase of H2 and CO in pyrolytic process of SCG, respectively, which is deemed to arise from enhanced thermal cracking of hydrocarbons and oxygen transfer reaction mediated by FO. Incorporation of FO successfully created porous structure in the produced biochar. The adsorption tests revealed that the biochar exhibited bi-functional capability to remove both positively charged Cd(II) and Ni(II), and negatively charged Sb(V). The adsorption of Cd(II) and Ni(II) was hardly deteriorated in the multiple adsorption cycles, and the adsorption of Sb(V) was further enhanced through formation of surface ternary complexes. The overall results demonstrated nano Fe(III) oxide is a promising amendment material in CO2-assisted pyrolysis of lignocellulosic biomass for enhancing syngas generation and producing functional biochar.

Multiple-functionalized biochar affects rice yield and quality via regulating arsenic and lead redistribution and bacterial community structure in soils under different hydrological conditions.

Rice grown in soils contaminated with arsenic (As) and lead (Pb) can cause lower rice yield and quality due to the toxic stress. Herein, we examined the role of functionalized biochars (raw phosphorus (P)-rich (PBC) and iron (Fe)-modified P-rich (FePBC)) coupled with different irrigation regimes (continuously flooded (CF) and intermittently flooded (IF)) in affecting rice yield and accumulation of As and Pb in rice grain. Results showed that FePBC increased the rice yield under both CF (47.4%) and IF (19.6%) conditions, compared to the controls. Grain As concentration was higher under CF (1.94-2.42 mg kg-1) than IF conditions (1.56-2.31 mg kg-1), whereas the concentration of grain Pb was higher under IF (0.10-0.76 mg kg-1) than CF (0.12-0.48 mg kg-1) conditions. Application of PBC reduced grain Pb by 60.1% under CF conditions, while FePBC reduced grain As by 12.2% under IF conditions, and increased grain Pb by 2.9 and 6.6 times under CF and IF conditions, respectively, compared to the controls. Therefore, application of the multiple-functionalized biochar can be a promising strategy for increasing rice yield and reducing the accumulation of As in rice grain, particularly under IF conditions, whereas it is inapplicable for remediation of paddy soils contaminated with Pb.

Iron-modified phosphorus- and silicon-based biochars exhibited various influences on arsenic, cadmium, and lead accumulation in rice and enzyme activities in a paddy soil.

Contamination of paddy soils with potentially toxic elements (PTEs) has become a severe environmental issue. Application of functionalized biochar for rice cultivation has been proposed as an effective means to reduce environmental risks of these PTEs in paddy soils. This work was undertaken to seek the positive effects of a rice husk-derived silicon (Si)-rich biochar (Si-BC) and a pig carcass-derived phosphorus (P)-rich biochar (P-BC), as well as their Fe-modified biochars (Fe-Si-BC and Fe-P-BC) on the enzyme activity and PTE availability in an As-Cd-Pb-contaminated soil. A rice cultivation pot trial was conducted using these functionalized biochars as soil amendments for the alleviation of PTE accumulation in rice plants. Results showed that Si-BC decreased the concentrations of As in rice grain and straw by 59.4 % and 61.4 %, respectively, while Fe-Si-BC significantly (P < 0.05) enhanced plant growth, increasing grain yield (by 38.6 %). Fe-Si-BC significantly (P < 0.05) elevated Cd and Pb accumulation in rice plants. P-BC enhanced the activities of dehydrogenase, catalase, and urease, and reduced grain-Pb and straw-Pb by 49.3 % and 43.2 %, respectively. However, Fe-P-BC reduced plant-As in rice grain and straw by 12.2 % and 51.2 %, respectively, but increased plant-Cd and plant-Pb. Thus, Fe-modified Si- and P-rich biochars could remediate paddy soils contaminated with As, and enhance the yield and quality of rice. Application of pristine P-rich biochar could also be a promising strategy to remediate the Pb-contaminated paddy soils and limit Pb accumulation in rice.

Chitin and crawfish shell biochar composite decreased heavy metal bioavailability and shifted rhizosphere bacterial community in an arsenic/lead co-contaminated soil.

Sustainable management of ever-increasing organic biowaste and arable soil contamination by potentially toxic elements are of concern from both environmental and agricultural perspectives. To tackle the waste issue of crawfish shells and simultaneously minimize the threat of arsenic (As) and lead (Pb) to human health, a pot trial was conducted using chitin (CT), crawfish shell biochar (CSB), crawfish shell powder (CSP), and CT-CSB composite to compare their remediation efficiencies in As/Pb co-contaminated soil. Results demonstrated that addition of all amendments decreased Pb bioavailability, with the greatest effect observed for the CT-CSB treatment. Application of CSP and CSB increased the soil available As concentration, while significant decreases were observed in the CT and CT-CSB treatments. Meanwhile, CT addition was the most effective in enhancing the soil enzyme activities including acid phosphatase, α-glucosidase, N-acetyl-ß-glucosaminidase, and cellobiohydrolase, whereas CSB-containing treatments suppressed the activities of most enzymes. The amendments altered the bacterial abundance and composition in soil. For instance, compared to the control, all treatments increased Chitinophagaceae abundance by 2.6-4.7%. The relative abundance of Comamonadaceae decreased by 1.6% in the CSB treatment, while 2.1% increase of Comamonadaceae was noted in the CT-CSB treatment. Redundancy and correlation analyses (at the family level) indicated that the changes in bacterial community structure were linked to bulk density, water content, and As/Pb availability of soils. Partial least squares path modeling further indicated that soil chemical property (i.e., pH, dissolved organic carbon, and cation exchange capacity) was the strongest predictor of As/Pb availability in soils following amendment application. Overall, CT-CSB could be a potentially effective amendment for simultaneously immobilizing As and Pb and restoring soil ecological functions in contaminated arable soils.

Review on distribution, fate, and management of potentially toxic elements in incinerated medical wastes.

Medical wastes include all solid and liquid wastes that are produced during the treatment, diagnosis, and immunisation of animals and humans. A significant proportion of medical waste is infectious, hazardous, radioactive, and contains potentially toxic elements (PTEs) (i.e., heavy metal (loids)). PTEs, including arsenic (As), cadmium (Cd), lead (Pb) and mercury (Hg), are mostly present in plastic, syringes, rubber, adhesive plaster, battery wastes of medical facilities in elemental form, as well as oxides, chlorides, and sulfates. Incineration and sterilisation are the most common technologies adopted for the safe management and disposal of medical wastes, which are primarily aimed at eliminating deadly pathogens. The ash materials derived from the incineration of hazardous medical wastes are generally disposed of in landfills after the solidification/stabilisation (S/S) process. In contrast, the ash materials derived from nonhazardous wastes are applied to the soil as a source of nutrients and soil amendment. The release of PTEs from medical waste ash material from landfill sites and soil application can result in ecotoxicity. The present study is a review paper that aims to critically review the dynamisms of PTEs in various environmental media after medical waste disposal, the environmental and health implications of their poor management, and the common misconceptions regarding medical waste.

Applications of agricultural residue biochars to removal of toxic gases emitted from chemical plants: A review.

Crop residues are representative agricultural waste materials, massively generated in the world. However, a large fraction of them is currently being wasted, though they have a high potential to be used as a value-added carbon-rich material. Also, the applications of carbon-rich materials from agricultural waste to industries can have economic benefit because waste-derived carbon materials are considered inexpensive waste materials. In this review, valorization methods for crop residues as carbon-rich materials (i.e., biochars) and their applications to industrial toxic gas removals are discussed. Applications of crop residue biochars to toxic gas removal can have significant environmental benefits and economic feasibility. As such, this review discussed the technical advantages of the use of crop residue biochars as adsorbents for hazardous gaseous pollutants and greenhouse gases (GHGs) stemmed from combustion of fossil fuels and the different refinery processes. Also, the practical benefits from the activation methods in line with the biochar properties were comprehensively discussed. The relationships between the physico-chemical properties of biochars and the removal mechanisms of gaseous pollutants (H2S, SO2, Hg0, and CO2) on biochars were also highlighted in this review study. Porosity controls using physical and chemical activations along with the addition of specific functional groups and metals on biochars have significantly contributed to the enhancement of flue gas adsorption. The adsorption capacity of biochar for each toxic chemical was in the range of 46-76 mg g-1 for H2S, 40-182 mg g-1 for SO2, 80-952 µg g-1 for Hg0, and 82-308 mg g-1 CO2, respectively. This helps to find suitable activation methods for adsorption of the target pollutants. In the last part, the benefits from the use of biochars and the research directions were prospectively provided to make crop residue biochars more practical materials in adsorption of pollutant gases.

Nitrate and ammonium ions removal from groundwater by a hybrid system of zero-valent iron combined with adsorbents.

Nitrate (NO(3)(-)) is a commonly found contaminant in groundwater and surface water. It has created a major water quality problem worldwide. The laboratory batch experiments were conducted to investigate the feasibility of HCl-treated zero-valent iron (Fe(0)) combined with different adsorbents as hybrid systems for simultaneous removal of nitrate (NO(3)(-)) and ammonium (NH(4)(+)) ions from aqueous solution. The maximum NO(3)(-) removal in combined Fe(0)-granular activated carbon (GAC), Fe(0)-filtralite and Fe(0)-sepiolite systems was 86, 96 and 99%, respectively, at 45 °C for 24 h reaction time. The NO(3)(-) removal rate increased with the increase in initial NO(3)(-) concentration. The NO(3)(-) removal efficiency by hybrid systems was in the order of sepiolite > filtralite > GAC. The NH(4)(+) produced during the denitrification process by Fe(0) was successfully removed by the adsorbents, with the removal efficiency in the order of GAC > sepiolite > filtralite. Results of the present study suggest that the use of a hybrid system could be a promising technology for achieving simultaneous removal of NO(3)(-) and NH(4)(+) ions from aqueous solution.

Pilot-scale passive bioreactors for the treatment of acid mine drainage: efficiency of mushroom compost vs. mixed substrates for metal removal.

Pilot-scale field-testing of passive bioreactors was performed to evaluate the efficiency of a mixture of four substrates (cow manure compost, mushroom compost, sawdust, and rice straw) relative to mushroom compost alone, and of the effect of the Fe/Mn ratio, during the treatment of acid mine drainage (AMD) over a 174-day period. Three 141 L columns, filled with either mushroom compost or the four substrate mixture (in duplicate), were set-up and fed with AMD from a closed mine site, in South Korea, using a 4-day hydraulic retention time. In the former bioreactor, effluent deterioration was observed over 1-2 months, despite the good efficiency predicted by the physicochemical characterization of mushroom compost. Steady state effluent quality was then noted for around 100 days before worsening in AMD source water occurred in response to seasonal variations in precipitation. Such changes in AMD quality resulted in performance deterioration in all reactors followed by a slow recovery toward the end of testing. Both substrates (mushroom compost and mixtures) gave satisfactory performance in neutralizing pH (6.1-7.8). Moreover, the system was able to consistently reduce sulfate from day 49, after the initial leaching out from organic substrates. Metal removal efficiencies were on the order of Al (∼100%) > Fe (68-92%) > Mn (49-61%). Overall, the mixed substrates showed comparable performance to mushroom compost, while yielding better effluent quality upon start-up. The results also indicated mushroom compost could release significant amounts of Mn and sulfate during bioreactor operation.

Sustainable valorization of styrofoam and CO2 into syngas.

Plastic is a versatile material broadly used in a variety of industries. However, the current disposal practices for plastic wastes (incineration/landfilling) add the hazardous materials into the environment. To offer a sustainable valorization platform for plastic waste, this study adopted the catalytic pyrolysis process using CO2 as a co-feedstock. A model plastic waste collected from a seaport was waste buoy (WB), which has been widely used in fishing industry. Prior to the pyrolysis tests, the exact type of plastic in WB and the thermolytic characteristics of WB were examined. Since the WB was made of polystyrene, it was mainly converted into styrene monomer (styrene), dimer (diphenyl-1-butene), and trimer (2,4,6-triphenyl-1-hexene) from pyrolysis of WB. To further valorize/detoxify styrene derivatives into value-added syngas, catalytic pyrolysis of WB was practiced using the Ni-based catalysts (2/5/10 wt% Ni/SiO2). The yield of H2 from the catalytic pyrolysis process of WB was more than one magnitude higher comparing to that from the non-catalytic one. H2 formation also increased as catalyst loading increased. When flow gas was switched from inert gas to CO2, CO gas formation was enhanced due to the chemical reactions between CO2 and styrene derivatives over Ni catalysts. Syngas (H2/CO) formation under the CO2 condition was 5 times higher in comparison to the N2 condition in catalytic pyrolyses of WB with 10 wt% Ni/SiO2. CO2 also effectively suppressed coke deposition on a Ni catalyst. This study proposes a sustainable valorization and disposal platform for used plastic waste and greenhouse gas (CO2), converting them into value-added fuel.